Pharmaceutical Validation SME (Chennai)

Note: This position is based out of Chennai. No remote option available.

Company Description

At Quascenta, we specialize in offering comprehensive validation lifecycle management software solutions. Our mission is to empower pharmaceutical manufacturing sites with the software tools they need to streamline their product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. Our flagship products, including eResiduePro, eProcessPro, and eLogBook, are designed to revolutionize how companies manage their product, process, and cleaning lifecycles. With over 20 years of experience, our solutions support organizations in meeting regulatory requirements while optimizing operations.

Role Description

This is a full-time on-site role in Chennai or a Pharmaceutical Validation SME. The candidate will be responsible for providing technical support to companies on the following software products:

• ValDoc Pro - Qualification lifecycle management software
• eLog Pro - Electronic logbook
• QMS Pro - Quality Management system software
• eResidue Pro - Cleaning validation software
• eProcess Pro - Process validation software

You will also be responsible for the following:

• Assist customers with uploading their SOPs and managing qualification in the application. Of interest to the customer will be the ability to execute qualification scripts (IQ/OQ/PQ) online
• Write test scripts and execute them. Open bug tickets where required.

Qualifications

• Prior experience using a QMS software, Validation role
• Experience in qualification of equipment/instruments
• Experience in process validation a plus